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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735023Generated: November 2, 2026

Formaldehyde → HCID 131719460, compound

https://huagongshe.com/reaction/1735023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-MethylpiperidineHCID 69381—
ReactantFumaric AcidHCID 444972—
ReactantHCID 15380030HCID 15380030—
CatalystCuprous chlorideHCID 62652—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131719460HCID 131719460—

Reaction Steps

A mixture of 1,2-dihydro-7-(2-propynyl)-benzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepin-6-one (4.45 gm, 16.2 mmole), paraformaldehyde (3.6 gm), 4-methylpiperidine (1.93 gm, 1.2 eq) and copper(I) chloride (300 mg), in dioxane (75 ml) was stirred for 16 hours at room temperature. After the reaction was complete, the mixture was diluted with dichloromethane (DCM, 300 ml). The insolubles were filtered off through a pad of celite. The solution was concentrated on a rotary evaporator to an oil (48 gm). The desired product was purified by flash chromatography over a silica gel column (100 gm, SiO2, eluted with 1% CH3OH:1% diethylamine:98% DCM, 1.5 l). The material obtained as a yellow syrup was dissolved in ether (50 ml) and filtered once. The ethereal solution was added to a solution of fumaric acid (1.9 gm, 1.0 eq) in ether (30 ml) with fast stirring. The salt crashed out as a thick gum. This mixture was diluted with ether (300 ml) and stirred for i hour, while the gum turned slowly to a solid. The solid was collected and recrystallized once from hot ethanol to afford yellow crystals: 3.9 gm, m.p. 157°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536717
Source datasetuspto-grants-1996_07
ORD IDord-d050ae3f4ea3459ca1e09b970bd40b72
Source noteuspto-grants-1996_07